Variant report

Variant	rs805261
Chromosome Location	chr6:31629211-31629212
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:57)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:57 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31627461-31629304	K562	blood:	n/a	n/a
2	POLR2A	chr6:31624845-31631075	K562	blood:	n/a	n/a
3	HEY1	chr6:31627241-31629259	K562	blood:	n/a	chr6:31628563-31628578
4	NR2F2	chr6:31627008-31629425	K562	blood:	n/a	n/a
5	POLR2A	chr6:31627859-31629233	U87	brain:	n/a	n/a
6	MAX	chr6:31627976-31629296	K562	blood:	n/a	n/a
7	CEBPB	chr6:31628082-31629224	K562	blood:	n/a	chr6:31628897-31628908
8	MBD4	chr6:31628122-31629259	HepG2	liver:	n/a	n/a
9	TEAD4	chr6:31625264-31629276	K562	blood:	n/a	n/a
10	HEY1	chr6:31628814-31629223	K562	blood:	n/a	n/a
11	POLR2A	chr6:31627704-31629224	K562	blood:	n/a	n/a
12	PML	chr6:31627400-31629252	K562	blood:	n/a	n/a
13	ELF1	chr6:31626778-31629307	K562	blood:	n/a	chr6:31628049-31628062
14	POLR2A	chr6:31626649-31630457	K562	blood:	n/a	n/a
15	MTA3	chr6:31627079-31629236	GM12878	blood:	n/a	n/a
16	POLR2A	chr6:31627492-31629239	U87	brain:	n/a	n/a
17	POLR2A	chr6:31627488-31629290	HL-60	blood:	n/a	n/a
18	POLR2A	chr6:31627885-31629241	K562	blood:	n/a	n/a
19	MAX	chr6:31626859-31629268	K562	blood:	n/a	n/a
20	POLR2A	chr6:31624936-31630633	HepG2	liver:	n/a	n/a
21	POLR2A	chr6:31624880-31629304	K562	blood:	n/a	n/a
22	SIN3AK20	chr6:31627064-31629219	K562	blood:	n/a	n/a
23	POLR2A	chr6:31624853-31630685	HepG2	liver:	n/a	n/a
24	POLR2A	chr6:31626622-31629281	HepG2	liver:	n/a	n/a
25	POLR2A	chr6:31626608-31630297	K562	blood:	n/a	n/a
26	POLR2A	chr6:31626356-31629360	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr6:31627844-31629253	HCT-116	colon:	n/a	n/a
28	POLR2A	chr6:31628228-31629331	SK-N-MC	brain:	n/a	n/a
29	POLR2A	chr6:31624894-31629292	K562	blood:	n/a	n/a
30	POLR2A	chr6:31627741-31629290	PFSK-1	brain:	n/a	n/a
31	EGR1	chr6:31628288-31629226	K562	blood:	n/a	chr6:31628563-31628576 chr6:31628604-31628626 chr6:31628610-31628621 chr6:31628609-31628622 chr6:31628609-31628622 chr6:31628565-31628575 chr6:31628950-31628965 chr6:31628563-31628576 chr6:31628609-31628622 chr6:31628564-31628578 chr6:31628566-31628575 chr6:31628563-31628576 chr6:31628610-31628619 chr6:31628563-31628577
32	FOSL2	chr6:31627549-31629337	HepG2	liver:	n/a	n/a
33	POLR2A	chr6:31627417-31629320	GM12892	blood:	n/a	n/a
34	POLR2A	chr6:31627684-31629270	K562	blood:	n/a	n/a
35	POLR2A	chr6:31627712-31629294	SK-N-SH	brain:	n/a	n/a
36	ARID3A	chr6:31627705-31629252	K562	blood:	n/a	n/a
37	MYBL2	chr6:31627325-31629235	HepG2	liver:	n/a	n/a
38	POLR2A	chr6:31626939-31629299	Hela-S3	cervix:	n/a	n/a
39	PML	chr6:31627396-31629308	K562	blood:	n/a	n/a
40	POLR2A	chr6:31627745-31629272	K562	blood:	n/a	n/a
41	POLR2A	chr6:31627770-31629219	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr6:31619380-31634380	HepG2	liver:	n/a	n/a
43	MBD4	chr6:31627724-31629227	HepG2	liver:	n/a	n/a
44	POLR2A	chr6:31628234-31629304	HCT-116	colon:	n/a	n/a
45	POLR2A	chr6:31627486-31630150	PFSK-1	brain:	n/a	n/a
46	HEY1	chr6:31624848-31631182	HepG2	liver:	n/a	chr6:31628563-31628578
47	POLR2A	chr6:31627611-31629854	PANC-1	pancreas:	n/a	n/a
48	CBX3	chr6:31627399-31629334	K562	blood:	n/a	n/a
49	POLR2A	chr6:31628822-31629253	HepG2	liver:	n/a	n/a
50	MYC	chr6:31627845-31629252	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31629199-31629249	AoSMC	blood vessel:	n/a
2	chr6:31629199-31629249	PrEC	prostate:	n/a
3	chr6:31629199-31629249	AG09309	skin:	n/a
4	chr6:31629199-31629249	NHBE	bronchial:	n/a
5	chr6:31629199-31629249	GM06990	blood:	n/a
6	chr6:31629199-31629249	HRCEpiC	kidney:	n/a
7	chr6:31629199-31629249	GM12891	blood:	n/a
8	chr6:31629199-31629249	IMR90	lung:	fetal
9	chr6:31629199-31629249	HEK293	kidney:	embryo
10	chr6:31629199-31629249	HEEpiC	esophagus:	n/a
11	chr6:31629199-31629249	Hela-S3	cervix:	n/a
12	chr6:31629199-31629249	GM12878	blood:	n/a
13	chr6:31629199-31629249	Hepatocyte	liver:	n/a
14	chr6:31629199-31629249	T-47D	breast:	n/a
15	chr6:31629199-31629249	LNCaP	prostate:	n/a
16	chr6:31629199-31629249	BE2_C	brain:	n/a
17	chr6:31629199-31629249	NH-A	brain:	n/a
18	chr6:31629199-31629249	ovcar-3	ovarian:	n/a
19	chr6:31629199-31629249	K562	blood:	n/a
20	chr6:31629199-31629249	AG09319	gingival:	n/a
21	chr6:31629199-31629249	AG04449	skin:	fetal
22	chr6:31629199-31629249	HL-60	blood:	n/a
23	chr6:31629199-31629249	SKMC	muscle:	n/a
24	chr6:31629199-31629249	HRPEpiC	eye:	n/a
25	chr6:31629199-31629249	U87	brain:	n/a
26	chr6:31629199-31629249	BJ	skin:	n/a
27	chr6:31629199-31629249	H1-hESC	embryonic stem cell:	embryo
28	chr6:31629199-31629249	AG04450	lung:	fetal
29	chr6:31629199-31629249	HNPCEpiC	eye:	n/a
30	chr6:31629199-31629249	GM19239	blood:	n/a
31	chr6:31629199-31629249	HepG2	liver:	n/a
32	chr6:31629199-31629249	PANC-1	pancreas:	n/a
33	chr6:31629199-31629249	NB4	blood:	n/a
34	chr6:31629199-31629249	HUVEC	blood vessel:	n/a
35	chr6:31629199-31629249	HMEC	breast:	n/a
36	chr6:31629199-31629249	HCT-116	colon:	n/a
37	chr6:31629199-31629249	ECC-1	luminal epithelium:	n/a
38	chr6:31629199-31629249	MCF10A-Er-Src	breast:	n/a
39	chr6:31629199-31629249	HCM	heart:	n/a
40	chr6:31629199-31629249	HAEpiC	amniotic membrane:	n/a
41	chr6:31629199-31629249	PFSK-1	brain:	n/a
42	chr6:31629199-31629249	HCF	heart:	n/a
43	chr6:31629199-31629249	CMK	blood:	n/a
44	chr6:31629199-31629249	ProgFib	skin:	n/a
45	chr6:31629199-31629249	AG10803	skin:	n/a
46	chr6:31629199-31629249	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:31629199-31629249	GM12892	blood:	n/a
48	chr6:31629199-31629249	HCPEpiC	choroid plexus:	n/a
49	chr6:31629199-31629249	A549	lung:	n/a
50	chr6:31629199-31629249	Jurkat	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31506029..31511048-chr6:31626239..31630287,7	MCF-7	breast:
2	chr6:31617566..31630444-chr6:31823885..31836000,84	K562	blood:
3	chr6:31625699..31629901-chr6:31762894..31764968,3	MCF-7	breast:
4	chr6:31586074..31595285-chr6:31626460..31635395,11	MCF-7	breast:
5	chr6:31508417..31511292-chr6:31625631..31629953,4	K562	blood:
6	chr6:31629136..31631208-chr6:31655120..31656869,2	MCF-7	breast:
7	chr6:31602610..31605344-chr6:31627504..31629558,2	MCF-7	breast:
8	chr6:31627970..31635325-chr6:31864036..31871429,12	K562	blood:
9	chr6:31628509..31634075-chr6:31935054..31938547,6	K562	blood:
10	chr6:31512487..31517874-chr6:31628889..31634381,12	K562	blood:
11	chr6:31629180..31631831-chr6:31863567..31866267,3	K562	blood:
12	chr11:65265197..65268056-chr6:31627481..31630298,2	MCF-7	breast:
13	chr12:109123761..109125995-chr6:31627199..31629495,2	MCF-7	breast:
14	chr6:31626270..31630199-chr6:31829030..31832230,7	K562	blood:

No data

Variant related genes	Relation type
CSNK2B	TF binding region
ENSG00000201207	TF binding region
C6orf47	TF binding region
ENSG00000263020	TF binding region
CSNK2B	CpG island
C6orf47	CpG island
ENSG00000201207	CpG island
ENSG00000263020	CpG island
ENSG00000204498	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000254870	Chromatin interaction
ENSG00000204427	Chromatin interaction
ENSG00000110880	Chromatin interaction
ENSG00000200816	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000204394	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204385	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000251562	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11576013	0.81[ASN][1000 genomes]
rs17201248	0.81[ASN][1000 genomes]
rs2142233	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2255741	0.91[AFR][1000 genomes]
rs2293852	0.93[ASN][1000 genomes]
rs2736158	0.83[AFR][1000 genomes]
rs2736161	0.86[AFR][1000 genomes]
rs2736165	0.84[AFR][1000 genomes]
rs28399972	0.87[ASN][1000 genomes]
rs2857696	0.86[AFR][1000 genomes]
rs61504963	0.81[ASN][1000 genomes]
rs707927	0.81[ASN][1000 genomes]
rs805258	0.87[AFR][1000 genomes]
rs805263	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs805264	0.91[AFR][1000 genomes]
rs805268	0.91[AFR][1000 genomes]
rs805270	0.91[AFR][1000 genomes]
rs805272	0.91[AFR][1000 genomes]
rs9469054	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
2	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
3	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
5	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
7	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
9	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
10	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
11	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
12	nsv884418	chr6:31525448-31741078	Active TSS Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
13	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
14	nsv462871	chr6:31575276-31632134	Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
15	nsv601942	chr6:31575276-31632134	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	133 gene(s)	inside rSNPs	diseases
16	nsv884419	chr6:31585000-31632651	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
17	nsv884420	chr6:31586827-31632651	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	138 gene(s)	inside rSNPs	diseases
18	nsv884421	chr6:31588151-31631907	Active TSS Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	129 gene(s)	inside rSNPs	diseases
19	nsv884422	chr6:31592524-31631907	Genic enhancers Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
20	nsv884424	chr6:31593729-31632651	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	93 gene(s)	inside rSNPs	diseases
21	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
22	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31627600-31629600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:31628600-31629600	Flanking Active TSS	Dnd41	blood
3	chr6:31628600-31631800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr6:31628800-31629400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:31628800-31629400	Enhancers	Lung	lung
6	chr6:31628800-31629600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr6:31628800-31629600	Enhancers	Spleen	Spleen
8	chr6:31628800-31630000	Weak transcription	Gastric	stomach
9	chr6:31629000-31629400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:31629000-31629400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr6:31629000-31629400	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr6:31629000-31629400	Enhancers	NH-A	brain
13	chr6:31629000-31629600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr6:31629000-31629600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:31629000-31629600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:31629000-31629600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:31629000-31629600	Enhancers	Liver	Liver
18	chr6:31629000-31629600	Enhancers	Colon Smooth Muscle	Colon
19	chr6:31629000-31629600	Enhancers	Fetal Brain Male	brain
20	chr6:31629000-31629600	Enhancers	HepG2	liver
21	chr6:31629000-31630000	Weak transcription	Aorta	Aorta
22	chr6:31629000-31630000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr6:31629000-31630200	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr6:31629000-31630200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr6:31629000-31631000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr6:31629000-31631000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr6:31629000-31631000	Weak transcription	HSMMtube	muscle
28	chr6:31629000-31631400	Weak transcription	Psoas Muscle	Psoas
29	chr6:31629000-31631600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:31629000-31631600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:31629000-31631600	Weak transcription	Ovary	ovary
32	chr6:31629000-31631800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr6:31629200-31629400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:31629200-31629400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:31629200-31629400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr6:31629200-31629400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:31629200-31629400	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr6:31629200-31629400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr6:31629200-31629400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr6:31629200-31629400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr6:31629200-31629400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:31629200-31629400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:31629200-31629400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr6:31629200-31629400	Enhancers	Fetal Lung	lung
45	chr6:31629200-31629400	Enhancers	Stomach Smooth Muscle	stomach
46	chr6:31629200-31629400	Enhancers	Thymus	Thymus
47	chr6:31629200-31629400	Enhancers	Hela-S3	cervix
48	chr6:31629200-31629400	Weak transcription	HSMM	muscle
49	chr6:31629200-31629400	Enhancers	NHLF	lung
50	chr6:31629200-31629600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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